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EUROIMMUN ANTI-PR3-HN-HR ELISA (IGG)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082130
510(k) Type
Traditional
Applicant
Euroimmun Us, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/2009
Days to Decision
252 days
Submission Type
Statement

EUROIMMUN ANTI-PR3-HN-HR ELISA (IGG)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082130
510(k) Type
Traditional
Applicant
Euroimmun Us, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/2009
Days to Decision
252 days
Submission Type
Statement